化学
一氧化氮介导的自由基聚合
星团(航天器)
分子内力
金属
铜
结晶学
酰胺
亲核细胞
配体(生物化学)
高分子化学
光化学
无机化学
立体化学
聚合
有机化学
聚合物
催化作用
自由基聚合
受体
程序设计语言
生物化学
计算机科学
作者
Ryu Tanimoto,Shuichi Suzuki,Masatoshi Kozaki,Yuki Kanzaki,Daisuke Shiomi,Kazunobu Sato,Takeji Takui,Rika Tanaka,Keiji Okada
标识
DOI:10.1002/slct.202002927
摘要
Abstract We prepared dicopper, disilver, and tetragold clusters ligated with (nitronyl nitroxide)‐substituted amidinate (NN‐amidinate). NN‐substituted amidine was prepared from N , N ′‐diphenylcarbodiimide via a nucleophilic reaction with nitronyl nitroxide as a radical anion. The NN‐amidinate ligand was generated by treatment with an appropriate base, and subsequent addition of copper(I), silver(I), or gold(I) sources gave the respective metal cluster systems of Cu 2 ‐(NN‐amidinate) 2 , Ag 2 ‐(NN‐amidinate) 2 , or Au 4 ‐(NN‐amidinate) 4 . These radical‐metal clusters exhibited excellent stability, even in solution under aerated conditions, making them easy to handle. Single crystals were obtained by recrystallization from suitable solvent systems. The spin structures of the cluster systems were investigated by ESR spectroscopy and magnetic susceptibility measurements, which indicated the existence of weak intramolecular, spin‐spin interactions between the NN moieties.
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